Difference between revisions of "Trazodone-escitalopram"
From Psychiatrienet
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| − | + | {{ Drugswitch | |
| + | | from = trazodone | ||
| + | | to = escitalopram | ||
| + | | stop = | ||
| + | * '''Before day 1:''' gradually reduce dosage of trazodone to a maximum of 150 mg/day, when this dosage is > 150 mg/day. | ||
| + | * '''Day 1:''' reduce dosage of trazodone to 75-100 mg/day. | ||
| + | * '''Day 8:''' stop administration of trazodone. | ||
| + | | start = | ||
| + | * A wash-out period is not necessary, but care is needed. | ||
| + | * '''Day 8:''' start administration of escitalopram in a normal dosage of 10 mg/day. | ||
| + | | info = | ||
| + | * Occurrence of serotonin syndrome is theoretically possible, so caution is necessary. | ||
| + | * Escitalopram is a weak inhibitor of CYP2D6, which metabolizes trazodone. | ||
| + | * The content of trazodone in the tablet, for example 100 mg or 150 mg, determines which exact doses are given. | ||
| + | }} | ||
Revision as of 23:54, 4 March 2010
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Switch medication from trazodone to escitalopram.[1] [2]
Stop trazodone - Before day 1: gradually reduce dosage of trazodone to a maximum of 150 mg/day, when this dosage is > 150 mg/day.
- Day 1: reduce dosage of trazodone to 75-100 mg/day.
- Day 8: stop administration of trazodone.
Start escitalopram- A wash-out period is not necessary, but care is needed.
- Day 8: start administration of escitalopram in a normal dosage of 10 mg/day.
More information- Occurrence of serotonin syndrome is theoretically possible, so caution is necessary.
- Escitalopram is a weak inhibitor of CYP2D6, which metabolizes trazodone.
- The content of trazodone in the tablet, for example 100 mg or 150 mg, determines which exact doses are given.
- ↑ Switches are based on literature references on this page and expert opinions of the authors. The authors have used pharmacokinetic and receptor affinity properties to determine the switch schedules
- ↑ Stahl, S. M. (2013). Stahl's essential psychopharmacology: Neuroscientific basis and practical applications (4th ed.). Cambridge University Press.
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